The role of IL-17 in systemic lupus erythematosus and its potential as a therapeutic target

被引:44
|
作者
Koga, Tomohiro [1 ,2 ]
Ichinose, Kunihiro [1 ]
Kawakami, Atsushi [1 ]
Tsokos, George C. [3 ]
机构
[1] Nagasaki Univ, Grad Sch Biomed Sci, Unit Adv Prevent Med Sci, Nagasaki, Japan
[2] Nagasaki Univ, Grad Sch Biomed Sci, Ctr Bioinformat & Mol Med, 1-12-4 Sakamoto, Nagasaki 8528523, Japan
[3] Harvard Med Sch, Beth Israel Deaconess Med Ctr, Dept Med, Div Rheumatol & Clin Immunol, Boston, MA 02115 USA
关键词
T cells; systemic lupus erythematosus (SLE); lupus nephritis; immune responses; interleukin (IL)-17; REGULATORY T-CELLS; PROTEIN-KINASE-IV; RESPONSE ELEMENT MODULATOR; GENOME-WIDE ASSOCIATION; MONOCLONAL-ANTIBODY; PHOSPHATASE; 2A; DOUBLE-BLIND; MECHANISTIC TARGET; GENE-EXPRESSION; TH17; CELLS;
D O I
10.1080/1744666X.2019.1593141
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Systemic lupus erythematosus (SLE) is an autoimmune disease characterized by autoantibodies production and immune complex deposition with systemic clinical manifestations. Interleukin (IL)-17-producing cells play a crucial role in disease pathogenesis and represent an attractive therapeutic target.Areas covered: This review provides an update on the possibility of targeting IL-17 in SLE. The rational for this approach as well as currently available and future targets are discussed.Expert opinion: Although human expression studies and animal models indicate that IL-17 blocking may be a promising therapeutic strategy for SLE, direct evidence for IL-17 inhibition in SLE patients is unavailable. Biologic therapies and small-molecule drugs that target IL-17 production are required for the achievement of a favorable clinical effect in SLE patients.
引用
收藏
页码:629 / 637
页数:9
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